The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
119620643 11962064 3 F 20151020 20160725 20160126 20160804 EXP CA-AMGEN-CANSP2012074066 AMGEN 61.00 YR A F Y 0.00000 20160804 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
119620643 11962064 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
119620643 11962064 2 SS HUMIRA ADALIMUMAB 1 Unknown 0
119620643 11962064 3 SS ORENCIA ABATACEPT 1 Unknown 0
119620643 11962064 4 SS ACTEMRA TOCILIZUMAB 1 Unknown 0
119620643 11962064 5 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown 400 MG, UNK 0 400 MG
119620643 11962064 6 SS NAPROXEN. NAPROXEN 1 Unknown UNK 0
119620643 11962064 7 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
119620643 11962064 8 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, BID 0 5 MG BID
119620643 11962064 9 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK, CYCLICAL 0
119620643 11962064 10 C METHOTREXATE. METHOTREXATE 1 20 MG, UNK 0 20 MG
119620643 11962064 11 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0
119620643 11962064 12 C FOLIC ACID. FOLIC ACID 1 0
119620643 11962064 13 C HCQ HYDROXYCHLOROQUINE SULFATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119620643 11962064 1 Rheumatoid arthritis
119620643 11962064 2 Rheumatoid arthritis
119620643 11962064 3 Rheumatoid arthritis
119620643 11962064 4 Rheumatoid arthritis
119620643 11962064 5 Rheumatoid arthritis
119620643 11962064 6 Rheumatoid arthritis
119620643 11962064 7 Rheumatoid arthritis
119620643 11962064 8 Rheumatoid arthritis
119620643 11962064 9 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
119620643 11962064 OT
119620643 11962064 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119620643 11962064 Arthropathy
119620643 11962064 C-reactive protein abnormal
119620643 11962064 Drug ineffective
119620643 11962064 Fall
119620643 11962064 Fatigue
119620643 11962064 Femur fracture
119620643 11962064 Impaired healing
119620643 11962064 Multiple fractures
119620643 11962064 Osteoporosis
119620643 11962064 Pain
119620643 11962064 Rash
119620643 11962064 Red blood cell sedimentation rate abnormal
119620643 11962064 Synovitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
119620643 11962064 5 2012 0
119620643 11962064 8 201011 20151115 0
119620643 11962064 9 2014 0
119620643 11962064 10 2012 2014 0